chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2062080806208081GA13GENIChomozygous45674282
2062080966208097TC16GENIChomozygous45674283
2062082206208221AG12GENIChomozygous45674284
2062084406208441CT20GENICpossibly homozygous45674285
2062096166209617TC20GENIChomozygous45674286
2062107206210721TC20GENICpossibly homozygous45674287